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| Term | familial hyperlipidemia | ID (Ontology) | DOID:1168 (Human Disease) |
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| Also Known As | "familial hyperlipoproteinemia" ; "hyperlipemia" | ||
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inherited metabolic disorder |__lipid metabolism disorder |__familial hyperlipidemia 21 rec. |__familial chylomicronemia syndrome 17 rec. | |__familial apolipoprotein A5 deficiency | |__familial apolipoprotein C-II deficiency | |__familial chylomicronemia due to inhibition of lipoprotein lipase activity | |__familial GPIHBP1 deficiency | |__familial lipase maturation factor 1 deficiency | |__familial lipoprotein lipase deficiency 17 rec. |__familial combined hyperlipidemia 17 rec. |__familial hypercholesterolemia 4 rec. | |__autosomal recessive hypercholesterolemia 1 rec. |__hyperlipoproteinemia type III |__hyperlipoproteinemia type IV |__hyperlipoproteinemia type V |
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| Is a | lipid metabolism disorder | ||
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ICD10CM:E78.5 MESH:D006949 MESH:D006951 NCI:C34707 NCI:C34709 SNOMEDCT_US_2023_03_01:154739000 SNOMEDCT_US_2023_03_01:3744001 UMLS_CUI:C0020473 UMLS_CUI:C0020476 |
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